Home Cart Sign in  
Chemical Structure| 1359857-62-7 Chemical Structure| 1359857-62-7

Structure of 1359857-62-7

Chemical Structure| 1359857-62-7

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 1359857-62-7 ]

CAS No. :1359857-62-7
Formula : C9H8BrFO2
M.W : 247.06
SMILES Code : O=C(OC)C1=C(F)C=CC(C)=C1Br
MDL No. :MFCD22987925

Safety of [ 1359857-62-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 1359857-62-7 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 1359857-62-7 ]

[ 1359857-62-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1359857-60-5 ]
  • [ 74-88-4 ]
  • [ 1359857-62-7 ]
YieldReaction ConditionsOperation in experiment
94% To a solution of 96 (1.53 g, 6.56 mmol) in DMF (30 mL) was added K2CO3 (2.26 g, 16.4 mmol, 2.5 equiv), and the mixture was stirred at rt for 10 min. MeI (0.815 mL, 13.1 mmol, 2 equiv) was added and then the reaction was stirred for 1 h, quenched with 1 N HCl and extracted with TBME. The organic phase was washed with saturated NaHCO3, brine and dried over anhydrous Na2SO4. The residue after rotary evaporation was purified by silica gel column chromatography to give 97 (1.5 g, 94%).
94% To a solution of <strong>[1359857-60-5]2-bromo-6-fluoro-3-methylbenzoic acid</strong> (52.7 g, 0.226 mol) in DMF (1000 mL) is added K2C03 (78.9 g, 0.57 mol), and the mixture is stirred at rt for 10 min before Mel (54.8 g, 0.45 mol) is added. The reaction is stirred for 1 h, quenched with 1 N HC1 (50 mL), diluted with water (500 mL) and extracted with EA (3 x 500 mL). The organic phase is washed with brine, dried over anhydrous Na2S04, filtered and concentrated under reduced pressure. The residue is purified by column chromatography using silica gel (30/1 to 10/1, v/v) to provide the desired product (52.3 g, yield 94%) as colorless oil.
 

Historical Records